Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g08890 | A08 | 8083236 | T | A | downstream_gene_variant | MODIFIER | c.*4983A>T| |
S39 |
2 | BAA08g08890 | A08 | 8089041 | C | T | intron_variant | MODIFIER | c.492-16G>A| |
S209 |
3 | BAA08g08890 | A08 | 8089626 | C | A | intron_variant | MODIFIER | c.109-25G>T| |
S157 S163 |
4 | BAA08g08890 | A08 | 8089801 | C | T | intron_variant | MODIFIER | c.109-200G>A| |
S105 S106 |
5 | BAA08g08890 | A08 | 8090187 | G | A | intron_variant | MODIFIER | c.109-586C>T| |
S39 |
6 | BAA08g08890 | A08 | 8090250 | G | A | intron_variant | MODIFIER | c.109-649C>T| |
S200 |
7 | BAA08g08890 | A08 | 8090359 | G | A | intron_variant | MODIFIER | c.109-758C>T| |
S247 |
8 | BAA08g08890 | A08 | 8090966 | G | A | intron_variant | MODIFIER | c.108+1060C>T| |
S125 |
9 | BAA08g08890 | A08 | 8091266 | C | T | intron_variant | MODIFIER | c.108+760G>A| |
S169 |
10 | BAA08g08890 | A08 | 8092224 | G | A | upstream_gene_variant | MODIFIER | c.-91C>T| |
S298 |
11 | BAA08g08890 | A08 | 8093831 | G | A | upstream_gene_variant | MODIFIER | c.-1698C>T| |
S160 |
12 | BAA08g08890 | A08 | 8095006 | G | A | upstream_gene_variant | MODIFIER | c.-2873C>T| |
S148 S210 |
13 | BAA08g08890 | A08 | 8095479 | G | A | upstream_gene_variant | MODIFIER | c.-3346C>T| |
S53 |
14 | BAA08g08890 | A08 | 8095583 | C | T | upstream_gene_variant | MODIFIER | c.-3450G>A| |
S155 S211 |
15 | BAA08g08890 | A08 | 8096093 | G | A | upstream_gene_variant | MODIFIER | c.-3960C>T| |
S11 S262 |
16 | BAA08g08890 | A08 | 8096232 | C | T | upstream_gene_variant | MODIFIER | c.-4099G>A| |
S144 |